US7579509B2 - Method and device for producing 1,2-dichlorethane by means of direct chlorination - Google Patents
Method and device for producing 1,2-dichlorethane by means of direct chlorination Download PDFInfo
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- US7579509B2 US7579509B2 US11/597,122 US59712205A US7579509B2 US 7579509 B2 US7579509 B2 US 7579509B2 US 59712205 A US59712205 A US 59712205A US 7579509 B2 US7579509 B2 US 7579509B2
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- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 title claims abstract description 72
- 238000000034 method Methods 0.000 title claims abstract description 21
- 238000005660 chlorination reaction Methods 0.000 title description 8
- 239000005977 Ethylene Substances 0.000 claims abstract description 69
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 68
- 238000006243 chemical reaction Methods 0.000 claims abstract description 64
- 239000000460 chlorine Substances 0.000 claims abstract description 48
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 46
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 45
- 230000003068 static effect Effects 0.000 claims abstract description 15
- 239000007788 liquid Substances 0.000 claims abstract description 13
- 238000007872 degassing Methods 0.000 claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 claims abstract description 7
- 239000012530 fluid Substances 0.000 claims abstract description 6
- 238000011144 upstream manufacturing Methods 0.000 claims abstract description 5
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 4
- 239000003054 catalyst Substances 0.000 claims abstract description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 238000009835 boiling Methods 0.000 description 9
- 239000007789 gas Substances 0.000 description 8
- IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 5
- 239000007791 liquid phase Substances 0.000 description 5
- 239000000376 reactant Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 238000000197 pyrolysis Methods 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000004581 coalescence Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- UBOXGVDOUJQMTN-UHFFFAOYSA-N 1,1,2-trichloroethane Chemical compound ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000002815 homogeneous catalyst Substances 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/20—Mixing gases with liquids
- B01F23/23—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids
- B01F23/232—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using flow-mixing means for introducing the gases, e.g. baffles
- B01F23/2323—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using flow-mixing means for introducing the gases, e.g. baffles by circulating the flow in guiding constructions or conduits
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/24—Stationary reactors without moving elements inside
- B01J19/2415—Tubular reactors
- B01J19/2435—Loop-type reactors
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/20—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles with liquid as a fluidising medium
- B01J8/22—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles with liquid as a fluidising medium gas being introduced into the liquid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
- C07C17/02—Preparation of halogenated hydrocarbons by addition of halogens to unsaturated hydrocarbons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
- B01F25/40—Static mixers
- B01F25/42—Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions
- B01F25/43—Mixing tubes, e.g. wherein the material is moved in a radial or partly reversed direction
- B01F25/431—Straight mixing tubes with baffles or obstructions that do not cause substantial pressure drop; Baffles therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/00796—Details of the reactor or of the particulate material
- B01J2208/00823—Mixing elements
- B01J2208/00831—Stationary elements
- B01J2208/0084—Stationary elements inside the bed, e.g. baffles
Definitions
- the invention relates to a process and a device for the production of 1,2-dichloroethane, hereinafter referred to as “EDC”, which primarily serves as an intermediate product in the production of monomer vinyl chloride, hereinafter referred to as “VCM”, which, in turn, is used to produce polyvinyl chloride (PVC). Hydrogen chloride HCl is obtained when EDC is reacted to produce VCM.
- EDC 1,2-dichloroethane
- VCM monomer vinyl chloride
- PVC polyvinyl chloride
- Hydrogen chloride HCl is obtained when EDC is reacted to produce VCM.
- the preferred method of producing EDC from ethylene C 2 H 4 and chlorine Cl 2 is such that a balance is maintained between the hydrogen chloride HCl produced and consumed in the various reactions shown below: Cl 2 +C 2 H 4 ⁇ C 2 H 4 Cl 2 (pure EDC)+218 kJ/Mole (1) C 2 H 4 Cl 2 (crackable EDC) ⁇ C 2 H 3 Cl (VCM)+HCl ⁇ 71 kJ/Mole (2) C 2 H 4 +2 HCl+1 ⁇ 2O 2 ⁇ C 2 H 4 Cl 2 (raw EDC)+H 2 O+238 kJ/Mole (3)
- balanced VCM process The process for the production of VCM with an adequate HCl balance, hereinafter referred to as “balanced VCM process”, comprises the following process steps:
- a circulating stream of EDC reaction product is used as the reaction fluid in the direct chlorination section.
- the circulating stream can be generated in a loop-type reactor with external or internal circulation system.
- the circulating stream can also be generated in a system with forced or natural circulation.
- ferric chloride is used as catalyst; in addition, sodium chloride, which can inhibit the formation of heavy ends, may be admixed as an additive.
- the state of the art as regards direct chlorination is, for instance, described in DE 199 10 964 A1.
- the process according to DE 199 10 964 A1 aims at suppressing side reactions, especially the continuation of the chlorination process of EDC to 1,1,2-trichlorethane, by letting most of the chlorination reaction to take place in the homogeneous liquid phase.
- the ethylene which is less readily soluble in EDC than chlorine, is completely dissolved in the main stream of the circulating EDC reaction fluid in a co-current bubble column.
- the chlorine which is more readily soluble in EDC than ethylene, is dissolved in a super-cooled EDC part-stream and the resulting solution of chlorine in EDC is fed to the circulating main stream which already contains the dissolved ethylene.
- Reaction ( 1 ) is usually run with a slight surplus of ethylene, in order to rule out corrosion problems in the reaction system, intensified formation of secondary products and problems involved in the treatment of chlorine-bearing waste gas streams.
- the reactor is supplied with a ratio-controlled feed of chlorine and ethylene, the ethylene content of the stream leaving the reactor serving as the control variable.
- the general aim for economical reasons is to minimise the surplus of ethylene at the reactor outlet in order to avoid excessive losses of ethylene.
- Reaction ( 1 ) in the subsequent reaction section proceeds kinetically according to a second-order velocity law. If both reactants initially have a stoichiometric ratio or if one reactant is in slight surplus, the reaction will proceed more slowly than it would if one reactant such as ethylene, for example, were initially present in a higher surplus in reaction ( 1 ). Transferred to a reactor of the type described herein, this means that the reaction is completed after a shorter run in the circulating reaction fluid stream than this would be the case with a lower initial surplus in ethylene.
- the aim of the present invention is to provide an economical process as well as a device which will permit an increase of the capacity without enlarging the external reactor dimensions while producing EDC of high purity.
- the aim can be achieved by:
- a further embodiment of the invention provides for supplying a highly hyper-stoichiometric amount of ethylene at all ethylene feed points except that of the last downstream admixing section. Feeding a 10 to 20% hyper-stoichiometric amount of ethylene has proved to be economically very efficient. Although the increased feed will make it necessary to accordingly enlarge the respective dissolving section, it will accelerate the reaction as a whole, which will result in a reduction of the overall height and allow additional feed points to be installed and the conversion rate to be improved.
- the boiling reactor according to the present invention is characterised by an excellent part-load performance, as it is possible to deactivate individual feed points even during operation, which is another advantage of the present invention. It is expedient to deactivate the upper feed points first and to lower the pressure so that the produced EDC can boil earlier. It is thus possible—even at low conversion rates—to compensate for the pressure loss caused by static mixers, if provided.
- the invention also refers to a device for implementing the process with a boiling reactor which consists of a degassing vessel, a reaction loop with natural circulation as well as discharge devices for the EDC produced and at least two feed devices each for dissolved chlorine and ethylene.
- the device may optionally also include static mixers.
- FIG. 1 shows a direct chlorination reactor consisting of degassing vessel 1 and loop 2 in which liquid EDC 3 , indicated by arrows, is circulated and which serves to run reaction ( 1 ), as well as the feed points for chlorine and ethylene according to the present invention.
- Gaseous pressurised ethylene 4 is distributed via control valves to ethylene feed points 5 , 6 and 7 .
- the ethylene feed points are designed so to produce fine bubbles, symbolically represented by dots in FIG. 1 , which can easily dissolve in the dissolving sections 8 , 9 and 10 .
- the dissolving sections 8 , 9 and 10 may optionally be equipped with static mixers 31 , 32 and 33 .
- the chlorine to be added is first dissolved in EDC.
- Part-stream 11 of the produced EDC is withdrawn from degassing vessel 1 and split into EDC stream 12 , which may also be an intermittent bleed stream, and solution stream 13 .
- Solution stream 13 is transferred by pump 14 to cooler 15 and subsequently to chlorine admixture point 16 where the gaseous chlorine 17 is added.
- Chlorine solution 18 is distributed at a controlled rate to chlorine feed points 19 , 20 and 21 and injected into loop 2 via a nozzle which produces the maximum possible turbulence.
- Reaction sections 22 , 23 and 24 which serve to run reaction ( 1 ) in the pure liquid phase are arranged downstream of chlorine feed points 19 , 20 and 21 . To improve the mixing quality, reaction sections 22 , 23 and 24 are equipped with static mixers 25 , 26 and 27 .
- reaction section 24 is followed by boiling section 28 , which is illustrated by bubbles in FIG. 1 .
- the vaporous EDC degasses into vapour chamber 29 of degassing vessel 1 from where it is discharged as vaporous EDC product 30 .
- Liquid EDC 3 is circulated at a rate of 8000 t/h in reaction loop 2 at a temperature of 90 to 135° C.
- Gaseous ethylene is fed to the loop via feed point 5 at a rate of 8892 kg/h, equivalent to 317 kmole/h, which dissolves in dissolving section 8 in the circulating EDC 3 .
- Liquid EDC (stream 13 ) is withdrawn at a rate of 1140 t/h from degassing vessel 1 , pumped through heat exchanger 15 by means of pump 14 , thereby being cooled to a temperature of between 30 and 60° C.
- gaseous or liquid chlorine is admixed to the cooled EDC stream at a rate of 61260 kg/h, equivalent to 864 kmole/h.
- the chlorine solution 18 thus obtained is split into three equal part-streams, each consisting of 380 t/h EDC and 20420 kg/h chlorine, equivalent to 288 kmole/h chlorine. These three part-streams are fed into the reactor loop via feed points 19 , 20 and 21 .
- the cooled EDC stream of 1140 t/h is first split into three equal part-streams of 380 t/h each, and 20420 kg/h, equivalent to 288 kmole/h, gaseous or liquid chlorine is admixed to each of these part-streams via separate chlorine admixing points.
- three part-streams of a solution of chlorine in EDC are obtained, each consisting of 380 t/h EDC and 20420 kg/h chlorine and which are fed into reactor loop 2 via feed points 19 , 20 and 21 .
- the first ethylene stream 5 as seen from bottom to top in the riser of the reactor loop, which has dissolved in section 8 in the circulating EDC stream 3 , is mixed with part-stream 19 of the chlorine-in-EDC solution.
- the reactants chlorine and ethylene react in the liquid phase along reaction section 22 , whereby EDC is formed.
- the reaction of the dissolved chlorine in fact proceeds more rapidly than if the reactants were present in equimolar quantities or if ethylene were only present with a small surplus.
- the reaction heat causes the circulating EDC 3 temperature to rise.
- the circulating EDC 3 which now enters the second ethylene dissolving section 9 , as seen from bottom to top in the riser of the reactor loop, will contain already dissolved ethylene.
- Dissolved ethylene is transferred at a rate, of 814 kg/h, equivalent to 29 kmole/h, with the EDC 3 into the ethylene dissolving section 9 .
- gaseous ethylene is fed via ethylene feed point 6 into the dissolving section at a rate of 8078 kg/h, equivalent to 288 kmole/h, which dissolves in the circulating EDC 3 along the ethylene dissolving section 9 .
- 8892 kg/h equivalent to 317 kmole/h dissolved ethylene is again contained in EDC 3 .
- part-stream 20 of chlorine dissolved in EDC is added to, and the chlorine and ethylene react to form EDC, along reaction section 23 .
- boiling of the reaction mixture is suppressed by the cooling action of the cooled chlorine solution stream and by an appropriate setting of the reactor pressure. Owing to the molar surplus of ethylene of 10%, the chlorine likewise reacts rapidly.
- dissolved ethylene is transferred at a rate of 814 kg/h, equivalent to 29 kmole/h, into the ethylene dissolving section 10 .
- Gaseous ethylene is fed via ethylene feed point 7 into the dissolving section at a rate of 7289 kg/h, equivalent to 260 kmole/h, which dissolves in the circulating EDC along the ethylene dissolving section 10 .
- reaction section 24 After passing through reaction section 24 , the hydrostatic pressure will decrease to an extent that the reaction mixture will start to boil and the reaction product can be withdrawn in gaseous state from degassing vessel 1 .
Abstract
Description
Cl2+C2H4→C2H4Cl2 (pure EDC)+218 kJ/Mole (1)
C2H4Cl2 (crackable EDC)→C2H3Cl (VCM)+HCl−71 kJ/Mole (2)
C2H4+2 HCl+½O2→C2H4Cl2 (raw EDC)+H2O+238 kJ/Mole (3)
-
- direct chlorination, in which one portion of the required EDC is produced from ethylene C2H4 and chlorine Cl2 in the presence of a homogeneous catalyst and made available as so-called pure EDC;
- oxychlorination, in which the remaining portion of the required EDC is produced from ethylene C2H4, hydrogen chloride HCl and oxygen O2 and made available as so-called raw EDC;
- fractionating EDC purification, in which the secondary products formed in the oxychlorination and EDC pyrolysis sections are removed from the raw EDC, the recycle EDC returned from the VCM fractionation section and, as an option, from the pure EDC in order to obtain a so-called feed EDC suitable for use in the EDC pyrolysis section; if desired, it is also possible to distil the pure EDC from the direct chlorination section in the heavy ends column of the EDC distillation section;
- EDC pyrolysis, in which the feed EDC is thermally cracked; the mixture leaving the reactor is the cracked gas which consists of VCM, hydrogen chloride HCl and non-reacted EDC as well as secondary products;
- VCM fractionation, in which the desired pure VCM product is separated from the cracked gas, while the other essential substances, viz. hydrogen chloride HCl and non-reacted EDC, contained in the cracked gas are recovered separately in the balanced VCM process and returned as recycle HCl or recycle EDC.
-
- a plurality of at least three admixing sections are arranged in the leg of the loop in which the liquid rises,
- each of these admixing sections has one upstream feed point for dissolved or gaseous ethylene and one downstream feed point for dissolved chlorine and may also have a static mixer.
Usually the feed point is designed as an injection nozzle, but it is also possible to choose a different design.
- 1 Degassing vessel
- 2 Loop
- 3 Liquid EDC
- 4 Ethylene
- 5 Ethylene feed point
- 6 Ethylene feed point
- 7 Ethylene feed point
- 8 Dissolving section
- 9 Dissolving section
- 710 Dissolving section
- 11 Part-stream
- 12 EDC stream
- 13 Solution stream
- 14 Pump
- 15 Cooler
- 16 Chlorine admixture
- 17 Gaseous chlorine
- 18 Chlorine solution
- 19 Chlorine feed point
- 20 Chlorine feed point
- 21 Chlorine feed point
- 22 Reaction section
- 23 Reaction section
- 24 Reaction section
- 25 Static mixer
- 26 Static mixer
- 27 Static mixer
- 28 Boiling section
- 29 Vapour chamber
- 30 Vaporous EDC product
- 31 Static mixer
- 32 Static mixer
- 33 Static mixer
Claims (2)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004029147A DE102004029147B4 (en) | 2004-06-17 | 2004-06-17 | Process and apparatus for the preparation of 1,2-dichloroethane by direct chlorination |
DE102004029147.0 | 2004-06-17 | ||
PCT/EP2005/006437 WO2005123635A1 (en) | 2004-06-17 | 2005-06-15 | Method and device for producing 1,2-dichlorethane by means of direct chlorination |
Publications (2)
Publication Number | Publication Date |
---|---|
US20080125613A1 US20080125613A1 (en) | 2008-05-29 |
US7579509B2 true US7579509B2 (en) | 2009-08-25 |
Family
ID=35115974
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/597,122 Active US7579509B2 (en) | 2004-06-17 | 2005-06-15 | Method and device for producing 1,2-dichlorethane by means of direct chlorination |
Country Status (13)
Country | Link |
---|---|
US (1) | US7579509B2 (en) |
EP (1) | EP1756026B1 (en) |
JP (1) | JP5419350B2 (en) |
KR (1) | KR101225389B1 (en) |
CN (2) | CN101555189A (en) |
AT (1) | ATE425944T1 (en) |
DE (2) | DE102004029147B4 (en) |
NO (1) | NO340146B1 (en) |
PL (1) | PL1756026T3 (en) |
RU (1) | RU2384556C2 (en) |
TW (1) | TWI491440B (en) |
UA (1) | UA88906C2 (en) |
WO (1) | WO2005123635A1 (en) |
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AU2005321593B2 (en) * | 2004-12-22 | 2011-11-03 | Thyssenkrupp Uhde Gmbh | Method for producing 1,2-dichloroethane by means of direct chlorination |
WO2015105911A1 (en) | 2014-01-08 | 2015-07-16 | Siluria Technologies, Inc. | Ethylene-to-liquids systems and methods |
US9133079B2 (en) | 2012-01-13 | 2015-09-15 | Siluria Technologies, Inc. | Process for separating hydrocarbon compounds |
US9328297B1 (en) | 2015-06-16 | 2016-05-03 | Siluria Technologies, Inc. | Ethylene-to-liquids systems and methods |
US9334204B1 (en) | 2015-03-17 | 2016-05-10 | Siluria Technologies, Inc. | Efficient oxidative coupling of methane processes and systems |
US9352295B2 (en) | 2014-01-09 | 2016-05-31 | Siluria Technologies, Inc. | Oxidative coupling of methane implementations for olefin production |
US9469577B2 (en) | 2012-05-24 | 2016-10-18 | Siluria Technologies, Inc. | Oxidative coupling of methane systems and methods |
WO2016205411A2 (en) | 2015-06-16 | 2016-12-22 | Siluria Technologies, Inc. | Ethylene-to-liquids systems and methods |
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US9944573B2 (en) | 2016-04-13 | 2018-04-17 | Siluria Technologies, Inc. | Oxidative coupling of methane for olefin production |
US10047020B2 (en) | 2013-11-27 | 2018-08-14 | Siluria Technologies, Inc. | Reactors and systems for oxidative coupling of methane |
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SE530767C2 (en) | 2006-10-03 | 2008-09-09 | Alfa Laval Corp Ab | Heat exchanger reactor with mixing zones and use of the heat exchanger reactor |
DE102008020386B4 (en) * | 2008-04-23 | 2012-01-26 | Uhde Gmbh | Apparatus and method for producing a chlorinated alkane |
DE102014214872A1 (en) * | 2014-07-29 | 2016-02-04 | Thyssenkrupp Ag | Process and apparatus for the synthesis of 1,2-dichloroethane |
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Citations (12)
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---|---|---|---|---|
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EP1756026B1 (en) | 2009-03-18 |
CN1984858A (en) | 2007-06-20 |
DE102004029147B4 (en) | 2008-01-03 |
UA88906C2 (en) | 2009-12-10 |
TW200610748A (en) | 2006-04-01 |
NO20070322L (en) | 2007-01-17 |
KR101225389B1 (en) | 2013-01-22 |
CN101555189A (en) | 2009-10-14 |
NO340146B1 (en) | 2017-03-13 |
WO2005123635A1 (en) | 2005-12-29 |
EP1756026A1 (en) | 2007-02-28 |
DE102004029147A1 (en) | 2006-01-12 |
KR20070028422A (en) | 2007-03-12 |
CN1984858B (en) | 2010-06-16 |
JP5419350B2 (en) | 2014-02-19 |
ATE425944T1 (en) | 2009-04-15 |
JP2008502632A (en) | 2008-01-31 |
TWI491440B (en) | 2015-07-11 |
DE502005006880D1 (en) | 2009-04-30 |
RU2384556C2 (en) | 2010-03-20 |
PL1756026T3 (en) | 2009-06-30 |
US20080125613A1 (en) | 2008-05-29 |
RU2007101533A (en) | 2008-07-27 |
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